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HRID 649作成日:2026年10月23日

N,N-Dimethylethylenediamine → N-(4-bromo-3-methoxyphenyl)-N',N'-dimethylethane-1,2-diamine

https://huagongshe.com/ja/reaction/649

反応式

関与物質

役割名称HCID仕込み量
反応物N,N-DimethylethylenediamineHCID 66053—
反応物1-Bromo-4-iodo-2-methoxybenzeneHCID 12187202—
試薬Sodium t-butoxideHCID 23676156—
触媒1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒TolueneHCID 1140—
生成物N-(4-bromo-3-methoxyphenyl)-N',N'-dimethylethane-1,2-diamineHCID 8286802045.64%

反応条件

温度80 °C

反応手順

A solution of 1-bromo-4-iodo-2-methoxybenzene (0.63 g, 2.01 mmol) dissolved in toluene (15.73 ml) was treated with N1,N1-dimethylethane-1,2-diamine (0.177 g, 2.01 mmol), SODIUM TERT-BUTOXIDE (0.232 g, 2.42 mmol), XANTPHOS (0.116 g, 0.20 mmol) and TRIS(DIBENZYLIDENEACETONE)DIPALLADIUM(0) (0.046 g, 0.05 mmol) under nitrogen. The resulting mixture was stirred at 80 °C in a sealed tube for 2 hours. The reaction mixture was diluted with water (200 mL), and extracted with ethyl acetate (200 mL). The organic was dried over MgSO4, filtered and evaporated to afford crude product. The crude product was purified by flash silica chromatography, elution 0-10% methanol in dcm. Pure fractions were evaporated to dryness to afford N1-(4-bromo-3-methoxyphenyl)-N2,N2-dimethylethane-1,2-diamine (0.251 g, 45.6 %) as a brown oil.

情報源と証拠

出典データセット750 AstraZeneca ELN dataset
ORD IDord-a7c71c7b356644fcbb6f6b90814539ca
出典メモ750 AstraZeneca ELN dataset